CROSS-REFERENCES TO RELATED APPLICATIONS
[0001] The present application is a continuation-in-part of
U.S. patent application Ser. No. 10/288,581 (Attorney Docket No. 018489-002540US), which is a continuation-in-part of
U.S. patent application Ser. No. 10/027,418, filed Dec. 19, 2001, entitled "Debulking Catheter", which claims the benefit of Provisional Patent Application
Serial No.
60/257,704, filed Dec. 20, 2000, entitled "Debulking Catheter" and Provisional Patent Application Serial No.
60/272,273 filed Feb. 27, 2001, entitled "Debulking Catheter", the complete disclosures of which are incorporated
herein by reference.
BACKGROUND OF THE INVENTION
[0002] The present invention is directed to devices and methods for cutting tissue. In a
specific application, the present invention is directed to devices and methods for
re-entering the true lumen from a subintimal space such as a dissection plane or so-called
"false lumen."
[0003] Guidewires and other interventional devices are used to treat vessels and organs
using endovascular approaches. A guidewire is typically guided through blood vessels
to the treatment site and the device is then advanced over the guidewire. For example,
angioplasty and stenting are generally accomplished by first introducing a guidewire
to the desired site and then advancing the angioplasty or stent catheter over the
guidewire.
[0004] When attempting to advance a guidewire or other interventional device through a highly
stenosed region or chronic total occlusion (CTO), the guidewire or device may inadvertently
enter into the wall of the vessel to create a sub-intimal space. Once in a sub-intimal
space, it can be difficult to re-enter the vessel true lumen. Devices for reentering
a vessel true lumen from a subintimal location are described in
WO 02/45598 which is hereby incorporated by reference.
BRIEF SUMMARY OF THE INVENTION
[0005] Various aspects of the invention are directed to methods and devices for re-entering
a lumen during an endovascular procedure. In one embodiment, the device has a cutter,
an opening, and an energy emitter coupled to the cutter. The device is advanced into
the subintimal space and energy is then emitted from the energy emitter to locate
the true lumen. In one aspect, the energy emitter and cutting element are moved together
which exposes the cutting element to cut an access path into the true lumen. In another
aspect of the present invention, the device may have a bendable tip which is bent
while cutting tissue to create the access path or may be bent to direct the device
or a guidewire through the access path.
[0006] In another aspect of the present invention, the device has a rotatable cutting element
which may be moved from a stored position to a cutting position which exposes over
180 degrees, and even 220 or even 270 degrees of the cutting element relative to the
axis of rotation. In another aspect of the invention, the cutter may be gradually
exposed as necessary. In still another aspect of the present invention, the body of
device may be wider along a portion of the device to urge tissue toward the cutting
element. The opening is relatively large and may be open at the distal end and may
expose at least part of the cutter at all positions distal to the opening. The open
end of the device permits the tissue to naturally move toward the cutter due to the
generally open nature of the distal end.
[0007] In still another aspect of the present invention, a system for accessing a subintimal
space includes a catheter through which the tissue cutting device is advanced. The
catheter may be coupled to a fluid source to inject contrast or the like and may also
be coupled to a pressure monitor for monitoring pressure to determine when the access
path has been created as described in greater detail below.
[0008] In a still further aspect of the invention, a method of entering a true lumen from
a false lumen during an endovascular procedure is provided. A guidewire is positioned
in the subintimal space. A reentry device is then advanced over the guidewire to the
target location in the subintimal space. The access path is then created using the
reentry device to cut the access path. The same guidewire is then directed through
the access path. The reentry device may have two different openings with the first
being used during advancement of the reentry device and a second opening through which
the guidewire extends when being directed through the access path. The first opening
may be configured to direct the guidewire substantially longitudinal while the second
opening directs the guidewire at an angle relative to the longitudinal axis.
[0009] These and other aspects of the invention will become apparent from the following
description, drawings and claims.
BRIEF DESCRIPTION OF THE DRAWINGS
[0010]
FIG. 1 shows a view of the system of the present invention.
FIG. 2 shows a guidewire positioned proximate to a total occlusion.
FIG. 3 shows a subintimal space created adjacent a true lumen by the guidewire.
FIG. 4 shows a reentry device of the present invention advanced over the guidewire
to the subintimal space.
FIG. 5 shows a guidewire positioned in the true lumen.
FIG. 6 shows the reentry device with the cutting element in a stored position.
FIG. 7 shows the reentry device with the cutting element in a cutting position.
FIG. 8 is a side view of the reentry device of FIG. 7.
FIG. 9 shows another reentry device with the cutting element in a stored position.
FIG. 10 shows the reentry device of FIG. 9 with the cutting element in a cutting position
and the distal portion bent.
FIG. 11 shows the reentry device of FIGS. 9 and 10 with the cutting element advanced
to another cutting position which exposes even more of the cutting element and also
bends the distal tip further.
FIG. 12 shows another reentry device which has a bendable distal portion.
FIG. 13 shows the reentry device of FIG. 12 with the distal portion bent.
FIG. 14 shows still another reentry device with a cutting element which may be tilted.
FIG. 15 shows the reentry device of FIG. 14 with the cutting element tilted to expose
more of the cutting element and to move the cutting element through the opening in
the body of the device.
FIG. 16 shows the reentry device of FIG. 6 having a junction leading to two separate
guidewire outlets with the guidewire positioned in the first outlet during advancement
of the device over the guidewire.
FIG. 17 shows the reentry device of FIG. 16 with the guidewire extending through the
second outlet for directing the guidewire into the true lumen.
FIG. 18 shows a catheter having a lumen for receiving a guidewire and another lumen
which receives the reentry device.
FIG. 19 shows another catheter having a single lumen through which the guidewire and
reentry device pass.
DETAILED DESCRIPTION OF THE INVENTION
[0011] Referring to FIGS. 1-8, a system 2 and device 4 for reentering a true lumen from
a subintimal space, dissection plane or so-called false lumen is shown. The device
4 includes a cutting element 6 coupled to a torque transmitting element 8, such as
a wire 10, which rotates the cutting element 6. The device 4 has an opening 12 at
a distal end 14 with the cutting element 6 movable between a stored position (FIG.
6) and a cutting position (FIGS. 7 and 8) which exposes the cutting element 6. The
cutting element 6 may be any suitable cutting element 6 such as the cutting element
6 described in patents incorporated by reference above. The cutting element 6 has
a circular cutting edge which has a diameter of about 1 mm although any suitable size
may be used depending upon the particular application. The cutting element 6 may also
be any other type of cutter such as a laser, ultrasound, RF or other type of cutter
without departing from various aspects of the present invention.
[0012] The device 4 has a flexible body 16 to navigate through blood vessels or other body
lumens to a target location. The body 16 may be made of any suitable material as is
known in the art such as Pebax. The torque transmitting element 8 extends through
a lumen 18 in the body 16. The body 16 may have more lumens for various reasons such
as introduction of fluids, such as contrast, or for delivery of another device 4 such
as a guidewire or interventional device. The torque transmitting element 8 is coupled
to a driver 20 which rotates the torque transmitting element 8 at a variable or fixed
speed.
[0013] The device 4 may also have an energy emitting element 22, such as an ultrasound element
25, which emits (and may receive) energy to determine the location of the true lumen
as explained below. The energy emitting element 22 is coupled to the cutting element
6 so that the energy emitting element 22 and cutting element 6 are rotated together.
The cutting element 6 is in the stored position when locating the true lumen so that
the cutting element 6 is not exposed and will not cut or damage tissue. The energy
emitting element 22 is positioned adjacent a window 24 which may be a side opening
26 or may simply be a portion of the sidewall which transmits a sufficient amount
of the energy therethrough. Any suitable energy emitting element 22 may be used such
as the ultrasound emitting element available from Boston Scientific and is marketed
under the name Atlantis(TM). The cutting element 6 may be mounted to a collar which
is then mounted to an ultrasound element holder 28 or the cutting element 6 may be
integrally formed with the ultrasound element holder 28.
[0014] The device 4 has an atraumatic tip 34 which is relatively flexible to prevent damaging
tissue. The tip 34 may be a separate piece laminated or glued to the body 16. The
tip 34 is preferably made out of a relatively soft, flexible material, such as tecothane,
and may be used for blunt dissection as necessary. A reinforcing element 36 is encapsulated
in the tip 34 to help the tip 34 maintain it's general shape. The tip 34 may also
have one or more guidewire lumens 38 or any of the guidewire features described herein.
[0015] The opening 12 in the distal portion may be designed to expose over 180 degrees of
the cutting element 6 and may even expose 220 degrees or even 270 degrees of the cutting
element 6 as defined by the axis of rotation. This provides advantages over
WO02/45598 which does not expose much of the cutting element 6 and requires invagination of
the tissue within the opening to cut tissue. In another aspect of the invention, the
cutting element 6 may be gradually exposed. For example, the cutting element 6 may
be gradually exposed from 180-220 degrees or even 200-270 degrees. As explained below,
this feature provides the user with the ability to change the amount of cutter 6 that
is exposed depending upon the tissue thickness between the subintimal location and
true lumen. The term opening 12 and amount of exposure of the cutting element 6 are
defined by the outer bounds of the opening 12 and the axis of rotation. Referring
to FIGS. 7 and 8, the cutting element 6 is exposed relative to the outer bounds of
the opening 12 due to the relatively open distal end.
[0016] Referring to FIGS. 9-11, another device 4A for reentering a true lumen from a subintimal
location is shown wherein the same or similar reference numbers refer to the same
or similar structure. The device 4A also has an opening 12A at the distal end to expose
the cutting element 6A. FIG. 9 shows the cutting element 6A in a stored position,
FIG. 10 shows the cutting element 6A in a first cutting position and FIG. 11 shows
the cutting element 6A in a second cutting position which further exposes the element
6A. The device 4A also has the window 24 through which the energy emitting element
22, such as the ultrasound element, may emit energy when the cutting element 6A is
in the stored position.
[0017] A distal portion 40 of the body can bend or articulate to further expose the cutting
element 6A and to move the cutting element 6A toward true lumen. The body has slots
42 formed therein to increase the flexibility of the distal portion 40. The cutting
element 6A has a surface 44 which engages a lip 46 on the body. As the cutting element
6A is advanced, the interaction between the surface 44 and lip 46 causes the distal
portion 40 to deflect. Bending the distal portion 40 can be helpful in moving the
cutting element 6A toward the tissue and may also expose more of the cutting element
6A. As also explained below, the tip 40 may also be bent to direct the device 4A itself
or a guidewire into the true lumen. The cutting element 6A may also be gradually exposed
as the cutting element 6A moves distally and may be gradually exposed in the same
manner described above.
[0018] Referring to FIGS. 12 and 13, another reentry device 4B is shown which has a distal
portion or tip 60 which bends or articulates. The tip 60 may be articulated and actuated
in any suitable manner. For example, the tip 60 may be bent upon longitudinal movement
of the cutting element 6 (as shown above) or a separate actuator, such as a pull wire
62, may be used. As can be appreciated from FIG. 13, the tip 60 is bent or articulated
to move the cutting element 6 toward the true lumen and to expose more of the cutting
element 6. The device 4B may also be bent to direct the device 4B itself or another
device or guidewire through the guidewire lumen 38 to the access path into the true
lumen as described further below.
[0019] Referring to FIGS. 14 and 15, still another device 4C for cutting tissue is shown
wherein the same or similar numbers refer to the same or similar structure. The device
4C includes a cutting element 6C, an energy emitting element 22C and a torque transmitter
8C for rotating the elements. The device 4C has an opening 64 along one side. The
cutting element 6C is contained within the opening 64 in the stored position of FIG.
14 and extends out of the opening 64 in the cutting position of FIG. 15. The cutting
element 6C is moved out of the window 24 using an actuator 68, such as a wire 70,
which tilts a bearing 72 supporting the shaft of the rotatable cutting element 6C.
Of course, any other suitable structure may be used to move the cutting element 6C
outside the opening 64 such as those described in
U.S. Pat. No. 6,447,525 which is hereby incorporated by reference. Furthermore, the cutting element 6C may
be moved out of the opening 64 by bending the distal portion or tip as described herein.
[0020] Use of the devices 4, 4A-C is now described with reference to the device 4 although
it is understood that any of the devices 4, 4A-C may be used. As mentioned above,
the device 4 may be used to perform any suitable procedure to cut from one location
to another in the body such as a procedure to reenter a true lumen. The device 4 is
initially advanced to a position within a subintimal space SS. As described above,
the subintimal space SS may be inadvertently created during an endovascular procedure
with a guidewire GW or other device creating the subintimal space SS as shown in FIGS.
2 and 3. The device 4 may be introduced over the same guidewire GW or device which
created the subintimal space SS as shown in FIGS. 4 and 5. Of course, the device 4
may also be advanced over the guidewire GW to a position proximate to the subintimal
space SS after which the device 4 is then advanced by itself into the subintimal space
SS.
[0021] After the device 4 is positioned at the appropriate location in the subintimal space
SS, the energy emitting element 22 is used to determine the location of the true lumen.
[0022] When using the ultrasound element 28, for example, the ultrasound element 28 is rotated
while emitting ultrasound energy and the energy emitted through the window 24 and
reflected back through the window 24 is processed as is known in the art. The entire
device 4 is rotated within the subintimal space SS to orient the window 24 until the
true lumen is located. The angular orientation of the device 4 is then maintained
so that the opening 12 and window 24 are directed toward the true lumen.
[0023] The cutting element 6 is then moved to the cutting position to expose the cutting
element 6. The cutting element 6 may be rotated with the driver 20 during this time
so that cutting is initiated as the cutting element 6 is exposed. In another aspect
of the invention, the entire device 4 itself may be moved through the subintimal space
to cut tissue. This provides advantages over the method of
WO 02/45598 which requires invagination of tissue through a window to attempt a cut at one location.
If the tissue does not invaginate sufficiently into the window, such as when the tissue
is too thick, the device of
WO 02/45598 will not be able to cut completely through the tissue to create the access path to
the true lumen. The user must then move the device and again attempt to invaginate
enough tissue to cut an access path. The present invention provides the ability to
move the entire device 4 through the subintimal space to create the access path rather
than attempting a cut at a single discrete location as in
WO 02/45598. Of course, the device 4 may also be used by moving only the cutting element 6 rather
than the entire device 4 without departing from the invention.
[0024] The cutting element 6 may also be exposed to varying degrees, as described above,
until enough of the cutting element 6 is exposed to cut through to the true lumen.
For example, the user may choose to expose half of the cutting element 6 and attempt
to create an access path to the true lumen. If an access path is not created, the
user may then choose to expose more of the cutting element 6 and again attempt to
create an access path. This procedure can be repeated until the access path is formed
to the true lumen. The device 4A, 4B may be also have a distal tip or portion 40,
60 which bends to move the cutting element 6 toward the tissue and/or expose more
of the cutting element 6 during cutting.
[0025] After successfully creating the access path into the true lumen, the device 4 itself
or part thereof may be directed toward or through the access path. Referring to FIG.
9-13, for example, the distal portion or tip 40, 60 may be bent to help direct the
device 4A, 4B itself or the guidewire GW through the access path.
[0026] Referring to FIGS. 16 and 17, another device 4D, similar to device 4, is shown which
has a guidewire lumen 74 having a junction 76 so the guidewire can be directed through
either a first lumen 77 having a first outlet 78 or a second lumen 79 having a second
outlet 80. The first outlet 78 directs the guidewire substantially longitudinally
for advancing the device 4D over the guidewire to the target area in a conventional
manner. The second outlet 80 directs the guidewire at an angle relative to the longitudinal
axis, such as 30-75 degrees, to direct the guidewire through the access path into
the true lumen.
[0027] The junction 76 may include a feature which directs the guidewire into the second
outlet 80. Referring to FIG. 17, for example, the junction 76 may include a flap or
stop 82 which closes and prevents or inhibits the guidewire from passing through the
first outlet 78 after the guidewire has been withdrawn proximal to the junction 76.
When the guidewire is advanced again as shown in FIG. 17, the guidewire passes through
the second outlet 80 due to the stop 82. The device 4 and/or guidewire GW are then
manipulated to direct the guidewire GW through the access path. Although the stop
82 may be provided, the junction 76 may also simply be a relatively open junction
76 with the user manipulating and rotating the guidewire GW to direct the guidewire
GW through the desired outlet 78, 80. The device is rotated about 180 degrees after
creating the access path to direct the GW through outlet 80 and into the true lumen.
[0028] Referring to FIGS. 18 and 19, the system 2 may also include a sheath or catheter
90 which is advanced proximal to the treatment site. The sheath 90 may help provide
better control of the guidewire GW and devices 4 of the present invention during manipulation
in the subintimal space. The sheath 90 may also used to deliver contrast solution
to the treatment site from a source of contrast 97 (see FIG. 1) or may be coupled
to a pressure sensor 94. The pressure sensor 94 may be part of the contrast delivery
system 97 or may be a separate component. Deliver of contrast and/or pressure monitoring
may be used to determine when the access path has been created. [
[0029] The sheath 90 may include only one lumen 92 with fluid delivery and pressure sensing
being accomplished in the annular space between the device and sheath as shown in
FIG. 19. The sheath 90 may also have first and second lumens 96, 98 for separate delivery
of the device 4 and guidewire GW. As mentioned above, the devices 4 of the present
invention may be advanced over the same guidewire or device that created the subintimal
space or may be advanced over another guidewire or even through the sheath 90 by itself.
[0030] After accessing the true lumen, another interventional device may be introduced into
the true lumen for the intended therapy or procedure. For example, a stent catheter,
angioplasty catheter, or atherectomy device may be used to treat the occlusion. The
present invention has been described for reentering a true lumen from a subintimal
space but, of course, may be used for other purposes to gain access from one space
to another anywhere within the body.
[0031] The present invention has been described in connection with the preferred embodiments,
however, it is understood that numerous alternatives and modifications can be made
within the scope of the present invention as defined by the claims.
1. An intravascular incising device (4, 4A, 4B, 4D), comprising:
an elongate body (16) having a distal portion (14, 40, 60), an opening (12, 12A) in
the distal portion (14, 40, 60), and at least one lumen (18), the body (16) being
sufficiently flexible to be advanced through a patient's vasculature to a treatment
site;
a torque transmitting element (8) extending through the lumen (18);
a cutting element (6, 6A) coupled to the torque transmitting element (8), the cutting
element (6, 6A) being movable relative to the opening (12, 12A) in the distal portion
(14, 40, 60) to a number of discrete positions to vary an amount of the cutting element
(6, 6A) which is exposed relative to the opening (12, 12A).
2. The device of claim 4, wherein:
the cutting element (6, 6A) is movable from a stored position in which the cutting
element (6, 6A) is not exposed to a working position where the cutting element (6,
6A) is exposed at least 180 degrees relative to the opening (12, 12A).
3. The device of claim 1, wherein:
the cutting element (6, 6A) is movable from a stored position in which the cutting
element (6, 6A) is not exposed to a working position where the cutting element (6,
6A) is exposed at least 220 degrees relative to the opening (12, 12A).
4. The device of claim 1, wherein:
the cutting element (6, 6A) is movable from a stored position in which the cutting
element (6, 6A) is not exposed to a working position where the cutting element (6,
6A) is exposed at least 270 degrees relative to the opening (12, 12A).
5. The device of claim 1, wherein:
the cutting element (6, 6A) may be gradually exposed between 180-220 degrees.
6. The device of claim 1, wherein:
the cutting element (6, 6A) may be gradually exposed between 200-270 degrees.
7. The device of claim 1, wherein:
the cutting element (6, 6A) may be moved longitudinally relative to the body (16)
for moving the cutting element (6, 6A) between the number of discrete positions.
8. The device of claim 2, further comprising:#
an energy emitting element (22) which emits energy to determine the location of a
body lumen.
9. The device of claim 8, wherein:
the energy emitting element (22) is coupled to the cutting element (6, 6A) so that
the energy emitting element (22) and the cutting element (6, 6A) are rotated together.
10. The device of claim 8, wherein:
the energy emitting element (22) is positioned adjacent a window (24) through which
the energy emitting element (22) may emit energy when the cutting element (6, 6A)
is in a stored position.
11. The device of claim 1, wherein:
the distal portion (14, 40, 60) is capable of bending to further expose the cutting
element (6, 6A).
12. The device of claim 11, wherein:
the distal portion (14, 40, 60) bends upon longitudinal movement of the cutting element
(6, 6A).
13. The device of claim 12, further comprising:
a lip (46) on the body (16),
wherein the cutting element (6, 6A) has a surface (44) which engages the lip on the
body (16) causing the distal portion (14, 40, 60) to bend upon longitudinal movement
of the cutting element (6, 6A).
14. The device of claim 11, further comprising:
an actuator (62) for bending the distal portion (14, 40, 60).
15. The device of claim 14, wherein:
the actuator comprises a pull wire (62).